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About This Item
Linear Formula:
H2NC6H3(CH3)CO2H
CAS Number:
Molecular Weight:
151.16
EC Number:
MDL number:
UNSPSC Code:
12352200
PubChem Substance ID:
NACRES:
NA.22
Recommended Products
Assay
98%
form
powder
reaction suitability
reaction type: solution phase peptide synthesis
mp
169-171 °C (lit.)
application(s)
peptide synthesis
SMILES string
Cc1cc(ccc1N)C(O)=O
InChI
1S/C8H9NO2/c1-5-4-6(8(10)11)2-3-7(5)9/h2-4H,9H2,1H3,(H,10,11)
InChI key
NHFKECPTBZZFBC-UHFFFAOYSA-N
Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
Target Organs
Respiratory system
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Regulatory Information
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Weixiang Liu et al.
Carbohydrate polymers, 160, 97-105 (2017-01-25)
A novel type of O-carboxymethyl chitosan Schiff bases (O-CSPX) was synthesized via a condensation reaction. After the coordination reaction of cupric ions, Cu(II) complexes (O-CSPX-Cu) were achieved. The theoretical structure of O-CSPX-Cu calculated by Gaussian 09 reveals that the copper
Chia-Ju Tsai et al.
Journal of chromatography. A, 1524, 29-36 (2017-10-11)
Detection of polar organic compounds (POCs) using gas chromatography (GC) is not straightforward due to high polarity, hydrophilicity, and low volatility of POCs. In this study, we report a tandem microwave-assisted derivatization method combined with salting-out assisted liquid-liquid microextraction (SALLME)
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